期刊论文详细信息
Respiratory Research
Early versus later response to treatment in patients with community-acquired pneumonia: analysis of the REACH study
Javier Garau6  Kyle McBride5  Jesús Medina1  Jill Racketa3  Helmut Ostermann2  Francesco Blasi4 
[1] Medical Evidence Centre (Global Medical Affairs), AstraZeneca, Parque Norte, Edificio Roble, Serrano Galvache 56, 28033 Madrid, Spain;Department of Internal Medicine III, Haematology and Oncology, University Hospital Munich, Munich, Germany;Health Economics and Outcomes Research, AstraZeneca, 1800 Concord Pike, 19850 Wilmington, DE, USA;Department of Pathophysiology and Transplantation, University of Milan, IRCCS Fondazione Ospedale Maggiore, Policlinico Cà Granda Milano, Italy;Instat Services, Inc., 1 Wilson Street, Chatham, NJ 07928 USA;Department of Medicine, Hospital Universitari Mutua de Terrassa, Plaza Doctor Robert 5, 08221 Terrassa, Barcelona, Spain
关键词: Resource use;    Early response;    Community-acquired pneumonia;    Clinical stability;   
Others  :  790788
DOI  :  10.1186/1465-9921-15-6
 received in 2013-07-04, accepted in 2014-01-17,  发布年份 2014
PDF
【 摘 要 】

Background

Key goals in the treatment of CAP include early response to treatment and achievement of clinical stability. The US FDA recommends early response endpoints (72 hours after initiation of treatment) in clinical trials for the treatment of community-acquired bacterial pneumonia. REACH (REtrospective Study to Assess the Clinical Management of Patients With Moderate-to-Severe Complicated Skin and Soft Tissue Infections [cSSTI] or CAP in the Hospital Setting) was a retrospective observational study, providing current data on the clinical management and resource burden of CAP in real-life settings in European hospitals. This analysis reviews the characteristics and outcomes of patients showing early positive response to treatment (time to clinical stability [TCS] ≤4 days, as assessed by Halm’s criteria) compared with patients with later positive response (TCS >4 days).

Methods

Patients were adults, hospitalized with CAP (2010–2011) and requiring in-hospital treatment with intravenous antibiotics.

Results

Of the 2039 patients included in REACH, 585 (28.7%) had TCS assessed by Halm’s criteria: 332 (56.8%) showed early response (median 3.0 days), and 253 (43.2%) showed later response to treatment (median 7.0 days). Use of Halm’s criteria varied across participating countries, ranging from 0% (Belgium) to 49.1% (UK). Patient characteristics and relevant medical history were similar between the two groups. There were no notable differences in initial antibiotic therapy between groups, except that more early responders had been treated with amoxicillin–clavulanate and amoxicillin monotherapy (22.6%; 7.5%, respectively) than later responders (5.9%; 1.2%, respectively). Initial treatment modification and re-infection or recurrences were less frequent in early responders compared with later responders (14.2% and 3.3% vs. 34.8% and 5.9%, respectively). Early responders had a shorter duration of hospitalization (mean 9.4 ± SD 7.0; median 8.0 days vs. mean 15.6 ± SD 10.5; median 12.0 days, respectively), lower rate of ICU admission (3.3% vs. 21.3%) and shorter duration of ICU stay (mean 6.2 ± SD 5.7; median 4.0 days vs. mean 10.4 ± SD 10.1; median 8.0 days, respectively) compared with later responders. Mortality was low in both groups.

Conclusions

Achieving early clinical stabilization in CAP (≤4 days) is associated with improved outcomes, lower requirement for initial treatment modification or readmission and lower resource use, compared with a later response.

Trial registration

NCT01293435

【 授权许可】

   
2014 Blasi et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140705003753198.pdf 231KB PDF download
【 参考文献 】
  • [1]Polverino E, Torres MA: Community-acquired pneumonia. Minerva Anestesiol 2011, 77:196-211.
  • [2]Martinez R, Reyes S, Lorenzo MJ, Menendez R: Impact of guidelines on outcome: the evidence. Semin Respir Crit Care Med 2009, 30:172-178.
  • [3]Blasi F, Garau J, Medina J, Ávila M, McBride K, Ostermann H: Current management of patients hospitalized with community-acquired pneumonia across Europe: outcomes from REACH. Respir Res 2013, 14:44. BioMed Central Full Text
  • [4]Woodhead M, Blasi F, Ewig S, Garau J, Huchon G, Ieven M, Ortqvist A, Schaberg T, Torres A, van der HG, Read R, Verheij TJ: Guidelines for the management of adult lower respiratory tract infections–full version. Clin Microbiol Infect 2011, 17(Suppl 6):E1-E59.
  • [5]Mandell LA, Wunderink RG, Anzueto A, Bartlett JG, Campbell GD, Dean NC, Dowell SF, File TM Jr, Musher DM, Niederman MS, Torres A, Whitney CG: Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis 2007, 44(Suppl 2):S27-S72.
  • [6]File TM Jr, Marrie TJ: Burden of community-acquired pneumonia in North American adults. Postgrad Med 2010, 122:130-141.
  • [7]File TM Jr, Wilcox MH, Stein GE: Summary of ceftaroline fosamil clinical trial studies and clinical safety. Clin Infect Dis 2012, 55(Suppl 3):S173-S180.
  • [8]Akash MS, Rehman K, Chen S: An overview of valuable scientific models for diabetes mellitus. Curr Diabetes Rev 2013, 9:286-293.
  • [9]Akash MS, Rehman K, Chen S: Role of inflammatory mechanisms in pathogenesis of type 2 diabetes mellitus. J Cell Biochem 2013, 114:525-531.
  • [10]Akash MS, Shen Q, Rehman K, Chen S: Interleukin-1 receptor antagonist: a new therapy for type 2 diabetes mellitus. J Pharm Sci 2012, 101:1647-1658.
  • [11]Welte T, Torres A, Nathwani D: Clinical and economic burden of community-acquired pneumonia among adults in Europe. Thorax 2012, 67:71-79.
  • [12]Rehman S, Rehman K, Akash MS: A prospective study of inpatients to determine microbial etiology and therapeutic outcome of antibiotics for community-acquired pneumonia in pakistan. Bioimpacts 2013, 3:91-95.
  • [13]Roson B, Carratala J, Fernandez-Sabe N, Tubau F, Manresa F, Gudiol F: Causes and factors associated with early failure in hospitalized patients with community-acquired pneumonia. Arch Intern Med 2004, 164:502-508.
  • [14]Halm EA, Fine MJ, Marrie TJ, Coley CM, Kapoor WN, Obrosky DS, Singer DE: Time to clinical stability in patients hospitalized with community-acquired pneumonia: implications for practice guidelines. JAMA 1998, 279:1452-1457.
  • [15]US Food Drug Administration: Endpoints and Clinical Trial Issues in Community-Acquired Bacterial Pneumonia. 2011. http://www.fda.gov/downloads/advisorycommittees/committeesmeetingmaterials/drugs/anti-infectivedrugsadvisorycommittee/ucm275823.pdf webcite
  • [16]Stone RA, Obrosky DS, Singer DE, Kapoor WN, Fine MJ: Propensity score adjustment for pretreatment differences between hospitalized and ambulatory patients with community-acquired pneumonia. Pneumonia Patient Outcomes Research Team (PORT) Investigators. Med Care 1995, 33:AS56-AS66.
  • [17]Ott SR, Hauptmeier BM, Ernen C, Lepper PM, Nuesch E, Pletz MW, Hecht J, Welte T, Bauer TT: Treatment failure in pneumonia: impact of antibiotic treatment and cost analysis. Eur Respir J 2012, 39:611-618.
  • [18]Aliberti S, Blasi F, Zanaboni AM, Peyrani P, Tarsia P, Gaito S, Ramirez JA: Duration of antibiotic therapy in hospitalised patients with community-acquired pneumonia. Eur Respir J 2010, 36:128-134.
  • [19]Krobot K, Yin D, Zhang Q, Sen S, Altendorf-Hofmann A, Scheele J, Sendt W: Effect of inappropriate initial empiric antibiotic therapy on outcome of patients with community-acquired intra-abdominal infections requiring surgery. Eur J Clin Microbiol Infect Dis 2004, 23:682-687.
  • [20]Aliberti S, Blasi F: Clinical stability versus clinical failure in patients with community-acquired pneumonia. Semin Respir Crit Care Med 2012, 33:284-291.
  • [21]Menendez R, Torres A: Treatment failure in community-acquired pneumonia. Chest 2007, 132:1348-1355.
  • [22]Menendez R, Torres A, Zalacain R, Aspa J, Martin-Villasclaras JJ, Borderias L, Benitez-Moya JM, Ruiz-Manzano J, de Castro FR, Blanquer J, Perez D, Puzo C, Sanchez-Gascon F, Gallardo J, Alvarez C, Molinos L: Guidelines for the treatment of community-acquired pneumonia: predictors of adherence and outcome. Am J Respir Crit Care Med 2005, 172:757-762.
  • [23]Menendez R, Torres A, Rodriguez DC, Zalacain R, Aspa J, Martin Villasclaras JJ, Borderias L, Benitez Moya JM, Ruiz-Manzano J, Blanquer J, Perez D, Puzo C, Sanchez-Gascon F, Gallardo J, Alvarez CJ, Molinos L: Reaching stability in community-acquired pneumonia: the effects of the severity of disease, treatment, and the characteristics of patients. Clin Infect Dis 2004, 39:1783-1790.
  • [24]Aliberti S, Peyrani P, Filardo G, Mirsaeidi M, Amir A, Blasi F, Ramirez JA: Association between time to clinical stability and outcomes after discharge in hospitalized patients with community-acquired pneumonia. Chest 2011, 140:482-488.
  • [25]Eckburg PB, Friedland HD, Llorens L, Smith A, Witherell GW, Laudano JB, Thye D: Day 4 clinical response of ceftaroline fosamil versus ceftriaxone for community-acquired bacterial pneumonia. Infect Dis Clin Pract 2012, 20:254-260.
  文献评价指标  
  下载次数:3次 浏览次数:9次